A Study to Learn About the Study Medicine Called Berobenatide (PF-08653944) in People With Overweight or Obesity
Pfizer · NCT07595549
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 954
- US sites recruiting
- 30
- Study start
- June 10, 2026
- Record last updated
- October 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this clinical study is to learn about the effects and safety of berobenatide (PF-08653944). This may help people with overweight or obesity lose weight. People in this study may also have type 2 diabetes.
About 950 adults will be in this study. Berobenatide will be compared to a placebo. A placebo does not have any medicine in it but looks just like the medicine being studied. Berobenatide or placebo is given by a shot under the skin in the belly area. The objective of the study is to compare the experiences of people receiving berobenatide to those of the people who do not to assess if the study medicine is effective and safe.
People will take part in this study for about 20 months. During this time, they will have about 15 study visits at the site. They will also have 2 study visits over the phone.
Being studied: PF-08653944; Placebo
Conditions: Obesity; Overweight and/or Obesity; Overweight
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Aged ≥18 years.
- BMI of: ≥30 kg/m2 or ≥27.0 kg/m2 to \<30.0 kg/m2 and must have at least 1 of the following weight-related co-morbidities: hypertension, dyslipidemia, obstructive sleep apnea, cardiovascular disease, or T2D.
Exclusion Criteria
- Have a self-reported body weight change greater than 5% within 90 days prior to Screening.
- Diagnosis of type 1 diabetes or any other form of diabetes other than T2D.
- History of acute or chronic pancreatitis.
- Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN-2).
Recruiting US locations
San Fernando Valley Health Institute
Canoga Park, CA 91304
Headlands Research California, LLC
Escondido, CA 92025
ImmuniMet, LLC
Modesto, CA 95350
Clinical Trials Research
Sacramento, CA 95821
University Clinical Investigators, Inc.
Tustin, CA 92780
Diablo Clinical Research, Inc.
Walnut Creek, CA 94598
Southern California Retina Specialists
West Hills, CA 91307
Nature Coast Clinical Research
Crystal River, FL 34429
West Coast Eye Institute
Lecanto, FL 34461
South Broward Research
Miramar, FL 33027
Center for Diabetes, Obesity and Metabolism Inc
Pembroke Pines, FL 33024
Cedar Crosse Research Center
Chicago, IL 60607
Northwestern University
Chicago, IL 60611
Endeavor Health - Family Medicine Administration
Evanston, IL 60201
Endeavor Health- Endocrinology Research
Skokie, IL 60077
MediSphere Medical Research Center, LLC
Evansville, IN 47714
Ascension Saint Agnes Heart Care
Baltimore, MD 21229
Aa Mrc Llc
Flint, MI 48504
University Of Nebraska Medical Center
Omaha, NE 68198
Albuquerque Clinical Trials, Inc.
Albuquerque, NM 87102
Weill Cornell Medicine - Comprehensive Weight Control Center
New York, NY 10021
Medication Management, LLC
Greensboro, NC 27401
Accellacare - Wilmington
Wilmington, NC 28401
Jeffrey Coleman, OD
Wilmington, NC 28401
Midwest Eye Center
Cincinnati, OH 45202
Velocity Clinical Research, Mt. Auburn
Cincinnati, OH 45219
PlanIt Research, LLC (Monitoring Room)
Houston, TX 77079
PlanIt Research, LLC
Houston, TX 77079
VIP Trials
San Antonio, TX 78230
York Clinical Research, LLC
Norfolk, VA 23504
Study contacts (from the official record)
- Pfizer CT.gov Call Center · 1-800-718-1021 · ClinicalTrials.gov_Inquiries@pfizer.com
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